This impurity is related to Cyproterone Acetate EP Impurity F is provided with comprehensive characterization data in accordance with regulatory guidelines. It is suitable for use in analytical method development, method validation (AMV), Quality Control (QC) applications for Abbreviated New Drug Applications (ANDA) and commercial production of Asenapine.
Cyproterone Acetate EP Impurity F is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:6-Chloro-17-hydroxy-1?,2?-dihydro-3?H-cyclopropa[1,2]-pregna-1,4,6-triene-3,20-dioneCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Cyproterone Molecular Formula: C22H27ClO3
Molecular Weight: 374.9
Storage: Store in a cool, dry place.